Sustained hydrostatic pressure tolerance of the shallow water shrimp Palaemonetes varians at different temperatures: Insights into the colonisation of the deep sea

2012 ◽  
Vol 162 (4) ◽  
pp. 357-363 ◽  
Author(s):  
Delphine Cottin ◽  
Alastair Brown ◽  
Andrew Oliphant ◽  
Nélia C. Mestre ◽  
Juliette Ravaux ◽  
...  
Keyword(s):  
Hydrostatic Pressure ◽  
Shallow Water ◽  
Deep Sea ◽  
Pressure Tolerance ◽  
Different Temperatures

scholarly journals Pressure tolerance of tadpole larvae of the Atlantic ascidian Polyandrocarpa zorritensis: potential for deep-sea invasion

2015 ◽  
Vol 63 (4) ◽  
pp. 515-520
Author(s):  
Paulo Yukio Gomes Sumida ◽  
Arthur Ziggiatti Güth ◽  
Miguel Mies
Keyword(s):  
Hydrostatic Pressure ◽  
Shallow Water ◽  
Vertical Migration ◽  
Deep Sea ◽  
Larval Mortality ◽  
Larval Stages ◽  
Ascidian Species ◽  
Pressure Tolerance ◽  
Settlement And Metamorphosis ◽  
Deep Sea Fauna

Abstract How deep-sea fauna evolved is a question still being investigated. One of the most accepted theories is that shallow water organisms migrated to deeper waters and gave origin to the deep-sea communities. However, many organisms are prevented from performing long vertical migrations by the increasing hydrostatic pressure. Tadpole larvae of the ascidian Polyandrocarpa zorritensis were submitted to pressure treatments of 1, 50, 100 and 200 atm. Survival, settlement and metamorphosis rates were verified after 24 hour incubation in a pressure chamber. The majority of larvae settled (84%, 62%, 83% and 77% respectively) and successfully underwent metamorphosis (93%, 59%, 85% and 60%) in all pressure treatments. Larval mortality was of less than 15% in all treatments, except for the 50 atm treatment, which presented 38% mortality. Nearly 100% of the surviving larvae underwent metamorphosis in the treatments of 1, 50 and 100 atm. However, 1/3 of the individuals were still in their larval stages in the 200 atm treatment and presented delayed development. These data suggest that ascidian larvae can withstand the hydrostatic pressure levels found in the deep-sea. It is therefore feasible that the current abyssal ascidian species may have colonized the deep-sea through vertical migration and in only a few generations.

scholarly journals Oxidation of trimethylamine to trimethylamine N-oxide facilitates high hydrostatic pressure tolerance in a generalist bacterial lineage

2021 ◽  
Vol 7 (13) ◽  
pp. eabf9941
Author(s):  
Qi-Long Qin ◽  
Zhi-Bin Wang ◽  
Hai-Nan Su ◽  
Xiu-Lan Chen ◽  
Jie Miao ◽  
...  
Keyword(s):  
Hydrostatic Pressure ◽  
Deep Sea ◽  
High Hydrostatic Pressure ◽  
Deep Ocean ◽  
Deep Sea Sediment ◽  
Growth And Survival ◽  
Tolerance Strategy ◽  
Bacterial Lineage ◽  
Pressure Tolerance ◽  
Genes Encoding

High hydrostatic pressure (HHP) is a characteristic environmental factor of the deep ocean. However, it remains unclear how piezotolerant bacteria adapt to HHP. Here, we identify a two-step metabolic pathway to cope with HHP stress in a piezotolerant bacterium. Myroides profundi D25T, obtained from a deep-sea sediment, can take up trimethylamine (TMA) through a previously unidentified TMA transporter, TmaT, and oxidize intracellular TMA into trimethylamine N-oxide (TMAO) by a TMA monooxygenase, MpTmm. The produced TMAO is accumulated in the cell, functioning as a piezolyte, improving both growth and survival at HHP. The function of the TmaT-MpTmm pathway was further confirmed by introducing it into Escherichia coli and Bacillus subtilis. Encoded TmaT-like and MpTmm-like sequences extensively exist in marine metagenomes, and other marine Bacteroidetes bacteria containing genes encoding TmaT-like and MpTmm-like proteins also have improved HHP tolerance in the presence of TMA, implying the universality of this HHP tolerance strategy in marine Bacteroidetes.

Gametogenesis and the reproductive cycle in the deep-sea anemone Paracalliactis stephensoni (Cnidaria: Actiniaria)

1990 ◽  
Vol 70 (1) ◽  
pp. 163-172 ◽  
Author(s):  
Michel Praet-Van
Keyword(s):  
Organic Matter ◽  
Shallow Water ◽  
Deep Sea ◽  
Phytoplankton Bloom ◽  
Sea Anemone ◽  
Bay Of Biscay ◽  
Sea Anemones ◽  
Spring Phytoplankton Bloom ◽  
Sea Floor ◽  
Ultrastructural Investigation

This ultrastructural investigation of gametogenesis in a deep-sea anemone of the Bay of Biscay trawled around 2000 m depth, contributes to the knowledge of biology and strategy of reproduction of deep-sea benthos.This sea anemone is dioecious. The sperm appears very similar to those of shallow water sea anemones of the genus, Calliactis. The ultrastructural investigation of oogenesis allows the characteristics of the stages of previtellogenesis and vitellogenesis to be defined. The latter begins with a period of lipogenesis correlated with the formation of a trophonema. Mature oocytes measure up to 180 (im in diameter. Study of spermatogenesis and oogenesis reveals that spawning occurs in April/May. In males, the main area of testicular cysts, full of sperm, reaches maximal development from March to May and, in females, the percentage of mature oocytes decreases from 33% in April to 1% in May.Spawning may be induced by the advent in the deep-sea of the products of the spring phytoplankton bloom. This period of spawning, during the increased deposition of organic matter to the deep-sea floor, may be an advantageous strategy for early development of Paracalliactis.

scholarly journals Dispersal and Differentiation of Deep-Sea Mussels of the GenusBathymodiolus(Mytilidae, Bathymodiolinae)

2009 ◽  
Vol 2009 ◽  
pp. 1-15 ◽  
Author(s):  
Akiko Kyuno ◽  
Mifue Shintaku ◽  
Yuko Fujita ◽  
Hiroto Matsumoto ◽  
Motoo Utsumi ◽  
...  
Keyword(s):  
Gene Flow ◽  
Genetic Differentiation ◽  
Shallow Water ◽  
Deep Sea ◽  
Dispersal Ability ◽  
Evolutionary Transition ◽  
Significant Genetic Differentiation ◽  
Evolutionary Processes ◽  
High Dispersal ◽  
High Gene

We sequenced the mitochondrial ND4 gene to elucidate the evolutionary processes ofBathymodiolusmussels and mytilid relatives. Mussels of the subfamily Bathymodiolinae from vents and seeps belonged to 3 groups and mytilid relatives from sunken wood and whale carcasses assumed the outgroup positions to bathymodioline mussels. Shallow water mytilid mussels were positioned more distantly relative to the vent/seep mussels, indicating an evolutionary transition from shallow to deep sea via sunken wood and whale carcasses.Bathymodiolus platifronsis distributed in the seeps and vents, which are approximately 1500 km away. There was no significant genetic differentiation between the populations. There existed high gene flow betweenB. septemdierumandB. breviorand low but not negligible gene flow betweenB. marisindicusandB. septemdierumorB. brevior, although their habitats are 5000–10 000 km away. These indicate a high adaptability to the abyssal environments and a high dispersal ability ofBathymodiolusmussels.

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